"70518-0336-1" National Drug Code (NDC)

Zithromax 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0336-1)
(REMEDYREPACK INC.)

NDC Code70518-0336-1
Package Description4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0336-1)
Product NDC70518-0336
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZithromax
Non-Proprietary NameAzithromycin Dihydrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170320
Marketing Category NameNDA
Application NumberNDA050784
ManufacturerREMEDYREPACK INC.
Substance NameAZITHROMYCIN DIHYDRATE
Strength500
Strength Unitmg/1
Pharmacy ClassesMacrolide Antimicrobial [EPC], Macrolides [CS]

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